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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 632566생성일: 2026년 10월 24일

2-(1-{[2,4-Bis(benzyloxy)-5-(prop-1-en-2-yl)phenyl]carbonyl}piperidin-4-yl)acetaldehyde → cyclopentyl N-[2-(1-{[2,4-dihydroxy-5-(propan-2-yl)phenyl]carbonyl}piperidin-4-yl)ethyl]-L-alaninate

https://huagongshe.com/ko/reaction/632566

반응식

참여 물질

역할이름HCID투입량
반응물2-(1-{[2,4-Bis(benzyloxy)-5-(prop-1-en-2-yl)phenyl]carbonyl}piperidin-4-yl)acetaldehydeHCID 86686420—
반응물L-Alanine, cyclopentyl ester, 4-methylbenzenesulfonate (1:1)HCID 86686421—
생성물cyclopentyl N-[2-(1-{[2,4-dihydroxy-5-(propan-2-yl)phenyl]carbonyl}piperidin-4-yl)ethyl]-L-alaninateHCID 54766821—

반응 단계

Prepared from Intermediate D and L-alanine cyclopentyl ester tosylate. 1H NMR (300 MHz, d3-MeOD) 6.96 (1H, s), 6.34 (1H, s), 5.34 (1H, m), 4.17 (2H, m), 4.07 (1H, m), 3.19 (3H, m), 2.98 (2H, t, J=12 Hz), 1.96 (2H, m), 1.93 (11H, m), 1.56 (3H, d, J=7.2 Hz), 1.29 (2H, m), 1.18 (6H, d, J=6.9 Hz). LC/MS: purity >98%, m/z 447.25 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321718B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-d09c7c2f2bfb4a1a818b1bdc696765f4
출처 메모uspto-grants-2016_04